Literature DB >> 21816470

Expression, adverse prognostic significance and therapeutic small molecule inhibition of Polo-like kinase 1 in multiple myeloma.

Robert P Evans1, Greg Dueck, Roger Sidhu, Sunita Ghosh, Inka Toman, Jonathan Loree, Nizar Bahlis, Alexander C Klimowicz, Joyce Fung, Michelle Jung, Raymond Lai, Linda M Pilarski, Andrew R Belch, Tony Reiman.   

Abstract

The amplified myeloma centrosome has been identified as a therapeutic target. The present study explored the expression and prognostic significance of the centrosome-associated protein PLK1 in myeloma and the effect of BI 2536, a potent and selective inhibitor of PLK1, on myeloma cells. High plasma cell expression of PLK1 protein in myeloma patient bone marrow biopsies is an independent adverse prognostic factor (HR=2.3, p=0.003 unadjusted; HR=1.9, p=0.03 in multivariable model). BI 2536 inhibits myeloma cell lines at nanomolar concentrations, and is therapeutic for xenografts in NOD/SCID mice. PLK1 inhibition is a potential new strategy for the treatment of multiple myeloma. Copyright Â
© 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21816470     DOI: 10.1016/j.leukres.2011.07.016

Source DB:  PubMed          Journal:  Leuk Res        ISSN: 0145-2126            Impact factor:   3.156


  10 in total

1.  Targeting polo-like kinase 1 suppresses essential functions of alloreactive T cells.

Authors:  Carsten Berges; Manik Chatterjee; Max S Topp; Hermann Einsele
Journal:  Immunol Res       Date:  2016-06       Impact factor: 2.829

2.  Validation of Polo-like kinase 1 as a therapeutic target in pancreatic cancer cells.

Authors:  Chao Zhang; Xiaodong Sun; Yuan Ren; Yunbo Lou; Jun Zhou; Min Liu; Dengwen Li
Journal:  Cancer Biol Ther       Date:  2012-08-15       Impact factor: 4.742

3.  Inhibiting Polo-like kinase 1 causes growth reduction and apoptosis in pediatric acute lymphoblastic leukemia cells.

Authors:  Stefanie A Hartsink-Segers; Carla Exalto; Matthew Allen; Daniel Williamson; Steven C Clifford; Martin Horstmann; Huib N Caron; Rob Pieters; Monique L Den Boer
Journal:  Haematologica       Date:  2013-06-10       Impact factor: 9.941

4.  Suppression of interferon β gene transcription by inhibitors of bromodomain and extra-terminal (BET) family members.

Authors:  Nazma Malik; Stefan Vollmer; Sambit Kumar Nanda; Marta Lopez-Pelaez; Alan Prescott; Nathanael Gray; Philip Cohen
Journal:  Biochem J       Date:  2015-04-20       Impact factor: 3.857

Review 5.  The therapeutic potential of cell cycle targeting in multiple myeloma.

Authors:  Anke Maes; Eline Menu; Kim De Veirman; Ken Maes; Karin Vand Erkerken; Elke De Bruyne
Journal:  Oncotarget       Date:  2017-06-28

6.  Evaluation of in vitro effects of various targeted drugs on plasma cells and putative neoplastic stem cells in patients with multiple myeloma.

Authors:  Katharina Blatt; Harald Herrmann; Gabriele Stefanzl; Wolfgang R Sperr; Peter Valent
Journal:  Oncotarget       Date:  2016-10-04

7.  Maternal embryonic leucine zipper kinase is a novel target for proliferation-associated high-risk myeloma.

Authors:  Arnold Bolomsky; Roy Heusschen; Karin Schlangen; Kathrin Stangelberger; Joséphine Muller; Wolfgang Schreiner; Niklas Zojer; Jo Caers; Heinz Ludwig
Journal:  Haematologica       Date:  2017-11-09       Impact factor: 9.941

8.  PLK1 gene suppresses cell invasion of undifferentiated thyroid carcinoma through the inhibition of CD44v6, MMP-2 and MMP-9.

Authors:  Xing-Guang Zhang; Xiao-Feng Lu; Xiu-Ming Jiao; Bin Chen; Jin-Xiao Wu
Journal:  Exp Ther Med       Date:  2012-09-28       Impact factor: 2.447

9.  Polo-like kinase 1 as target for cancer therapy.

Authors:  Lily Weiß; Thomas Efferth
Journal:  Exp Hematol Oncol       Date:  2012-12-10

Review 10.  Kinase inhibitors as potential agents in the treatment of multiple myeloma.

Authors:  Hanley N Abramson
Journal:  Oncotarget       Date:  2016-12-06
  10 in total

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